The effect of the dilution rate on CHO cell physiology and recombinant interferon‐γ production in glucose‐limited chemostat culture
- 5 November 1993
- journal article
- research article
- Published by Wiley in Biotechnology & Bioengineering
- Vol. 42 (9) , 1077-1085
- https://doi.org/10.1002/bit.260420909
Abstract
The physiology of a recombinant Chinese hamster ovary cell line in glucose-limited chemostat culture was studied over a range of dilution rates (D = 0.008 to 0.20 h−1). The specific growth rate (μ) deviated from D at low dilution rates due to an increased specific death rate. Extrapolation of these data suggested a minimum specific growth rate of 0.011 h−1 (μmax = 0.025 h−1) The metabolism at each steady state was characterized by determining the metabolic quotients for glucose, lactate, ammonia, amino acids, and interferon-γ (IFN-γ). The specific rate of glucose uptake increased linearly with μ, and the saturation constant for glucose (Ks) was calculated to be 59.6 μM. There was a linear increase in the rate of lactate production with a higher yield of lactate from glucose at high growth rates. The decline in the rate of production of lactate, alanine, and serine at low growth rate was consistent with the limitation of the glycolytic pathway by glucose. The specific rate of IFN-γ production increased with μ in a manner indicative of a growth-related product. Despite changes in the IFN-γ production rate and cell physiology, the pattern of IFN-γ glycosylation was similar at all except the lowest growth rates where there was increased production of nonglycosylated IFN-γ. © 1993 John Wiley & Sons, Inc.Keywords
This publication has 36 references indexed in Scilit:
- Cell cycle model for growth rate and death rate in continuous suspension hybridoma culturesBiotechnology & Bioengineering, 1992
- Effects of glucose on the production of recombinant protein C in mammalian cell cultureBiotechnology & Bioengineering, 1992
- Glucose‐limited chemostat culture of chinese hamster ovary cells producing recombinant human interferon‐γBiotechnology & Bioengineering, 1992
- The effect of specific growth rate and death rate on monoclonal antibody production in hybridoma chemostat culturesThe Canadian Journal of Chemical Engineering, 1991
- Kinetic study of hybridoma cell growth in continuous culture. I. A model for non‐producing cellsBiotechnology & Bioengineering, 1991
- Transient expression of a p58 protein kinase cDNA enhances mammalian glycosyltransferase activityBiochemical and Biophysical Research Communications, 1990
- Cultivation of hybridoma cells in continuous cultures: Kinetics of growth and product formationBiotechnology & Bioengineering, 1989
- A kinetic analysis of hybridoma growth and metabolism in batch and continuous suspension culture: Effect of nutrient concentration, dilution rate, and pHBiotechnology & Bioengineering, 1988
- Reduction of waste product excretion via nutrient control: Possible strategies for maximizing product and cell yields on serum in cultures of mammalian cellsBiotechnology & Bioengineering, 1986
- Characteristics of the chemostat culture of murine leukemia L 1210 cellsExperimental Cell Research, 1976